Canonical Allele Identifier: PA202127
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192152
ClinVar RCV Id: RCV000172632 RCV000176834 RCV000769938 RCV001086126 RCV001840213 RCV002336415 RCV001293185 RCV001840210 RCV001840211 RCV001840212 RCV004539590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr24897Ala
CA202125
NM_001256850.1:c.74689A>G